Townsend Farms Inc Recall: Potential to be contaminated with Listeria monocytogenes.

🇺🇸 United States

1. June 21, 2023 - Recall initiated
2. July 26, 2023 - Reported by source
3. October 6, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1273-2023

Event ID

92623

Status

Terminated

Classification

Class I

Company

Townsend Farms Inc

Product description

Private Selection 48oz Tropical Mango Chunks, frozen product, 8/48 oz bags per case. UPC 0 11110 84663 1. Distributed by The Kroger Co. Cincinnati, OH

Quantity

79,656 bags (48oz. per bag)

Reason

Potential to be contaminated with Listeria monocytogenes.

Recall initiation date

June 21, 2023

Report date

July 26, 2023

Classification date

Not published in this source record

Termination date

October 6, 2023

Distribution pattern

Distributed in Alabama, Arkansas, Georgia, Illinois, Indiana, Kentucky, Louisiana, Michigan, Missouri, Mississippi, Ohio, South Carolina, Tennessee, Texas, Virginia, and West Virginia.

UPC, lot, and code information

BEST IF USED BY: 04/30/24 05/04/24 05/07/24 07/18/24 CODES: 04/30/24 T1 PRODUCT OF MEXICO F2202171 04/30/24 T1 PRODUCT OF MEXICO F2202182 04/30/24 T2 PRODUCT OF MEXICO F2202172 04/30/24 T2 PRODUCT OF MEXICO F2202183 05/04/24 T1 PRODUCT OF MEXICO F2202225 05/04/24 T1 PRODUCT OF MEXICO F2202229 05/07/24 T4 PRODUCT OF MEXICO F2202236 05/07/24 T4 PRODUCT OF MEXICO F2202241 07/18/24 T3 PRODUCT OF MEXICO F2300116

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 92623 with 3 other product entries in Public Health Trace.

Responsible company: Townsend Farms Inc

Other recalls from Townsend Farms Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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